Heteroareno-annelated estranes by triene cyclization

Masataka Watanabe, Taisuke Matsumoto, Shuntaro Mataka, Thies Thiemann

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

17-Thienyl-and 17-benzo[b]thienyl-3-hydroxyestra-1,3,5(10),16-tetraenes were synthesized by either sequential or one-pot Suzuki cross-coupling and Wittig olefination reactions. At 160 °C, heteroaryl substituted steroids were observed to undergo thermal intramolecular cyclization to produce E-ring heteroareno-annelated estranes.

Original languageEnglish
Pages (from-to)375-402
Number of pages28
JournalCentral European Journal of Chemistry
Volume4
Issue number3
DOIs
Publication statusPublished - Sep 2006
Externally publishedYes

Keywords

  • Annelation
  • Cyclization
  • Steroids
  • Trienes

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Chemistry

Fingerprint

Dive into the research topics of 'Heteroareno-annelated estranes by triene cyclization'. Together they form a unique fingerprint.

Cite this